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| Experimental Information | |
| Enzymatic Activity | |
| Molecule Id | EGIN0000002 |
| PMID | 18702009 |
| Assay Used | Sigma Kit ( Enzyme assay) |
| Experimently Validated | Yes |
| EGFR (IC50) | - |
| HER2 (IC50) | - |
| HER4 (IC50) | - |
| Mutant L858R (IC50) | - |
| Mutant T790M (IC50) | - |
| Double Mutant (IC50) | - |
| Average ERBB2 and ERBB1 (IC50) | - |
| Inhibition EGFR (%) | 78% , 86% |
| Inhibitory Concentration | 10然 and 30然 |
| Inhibition HER2 (%) | - |
| Inhibitory Concentration | - |
| Ki (EGFR) | - |
| Ki (HER2) | - |
| Ki (HER4) | - |
| Kd (EGFR) | - |
| Kd (L858R) | - |
| Kd (T790M) | - |
| Kd (L858R/T790M) | - |
| Kd (Other mutation) | - |
| Note | The paper describes the Synthesis and Characterization of Novel Quinazoline Type Inhibitors for Mutant and Wild-Type EGFR and RICK Kinases |
| Extra | 100,100(% inhibition 10然 and 30然,DL-EGFR),97,99(% inhibition 10然 and 30然,LR-EGFR),0,0(% inhibition 10然 and 30然,LR/TM-EGFR) |
| Cellular Activity | ||||||||||||||
| S.No. | Cell Line | Desp. | IC50 | IC80 | ED50 | GI50 | GI90 | EC50 | Kd | Inhibition (%) | Inhibitory Conc. | |||
| 1 | - | - | - | - | - | - | - | - | - | - | - | |||
| Activity against Receptor | |
| EGFR | Yes |
| HER2 | - |
| HER4 | - |
| Wild type | Yes |
| Mutant | delL747-P753insS , L858R , L858R/T790M |
| Inhibitor Binding | |
| EGFR | - |
| HER2 | - |
| HER4 | - |